子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 41 | Process for dyeing and printing cellulose esters and cellulose ethers | US18535527 | 1927-04-20 | US1765142A | 1930-06-17 | ERICH FISCHER; ERICH MULLER CARL |
| 42 | 메탈릭사와 폴리에스테르사를 원료로 이용한 편직물의 염색 방법 및 이러한 방법으로 제조된 편직물 | KR1020110118196 | 2011-11-14 | KR101145879B1 | 2012-05-15 | 우정하; 김선진; 조성현 |
| 본 발명은 메탈릭사와 폴리에스테르사를 원료로 이용한 편직물의 염색 방법 및 이러한 방법으로 제조된 편직물에 관한 것으로, 자세하게는 메탈릭사 및 400~600kg/mm
2 의 탄성율과 30 ~ 40%의 신장도를 갖는 상압 염색 폴리에스테르사를 원료로 사용하여 편직물을 직조하는 직조단계; 염료를 물에 분산시킨 염료용액을 투입하여 염욕을 제조하는 염욕제조단계; 상기 직조된 편직물을 상기 제조된 염욕에 투입하여, 염욕의 온도를 35 ~ 45℃에서부터 1.2 ~ 1.5℃/분의 속도로 30 ~ 50분간 높이고, 상기 승온된 염욕을 90 ~ 100℃에서 15 ~ 25분간 유지하여 상기 편직물을 염착하는 단계; 및 상기 염착된 편직물을 수세하는 단계;를 포함하는 염색된 편직물의 제조방법에 대한 것이다. 이렇게 제조된 염색된 편직물은 20% ~ 30%의 광반사 감소율을 갖는다.
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| 43 | 오염방지와 빠른 건조를 위한 폴리에스테르 섬유의제조방법 | KR1020080055628 | 2008-06-13 | KR1020090129613A | 2009-12-17 | 이원무 |
| PURPOSE: A manufacturing method of polyester fiber having quick-drying property and anti-fouling property is provided to remove foreign materials attached on the fiber easily with water, and to increase moisture absorption of the polyester fiber. CONSTITUTION: A manufacturing method of polyester fiber having quick-drying property and anti-fouling property includes the following steps of: mixing water and materials based on the polyester fiber and a benzenedicarboxylic composite material; combining a fiber finishing material with the mixed water; and drying the combined fiber finishing agent for 1 minute in 170 °C. | ||||||
| 44 | TREATMENT LIQUID COMPOSITION FOR INK JET PIGMENT TEXTILE PRINTING, TREATMENT LIQUID COMPOSITION SET FOR INK JET PIGMENT TEXTILE PRINTING, AND INK JET TEXTILE PRINTING METHOD | US16261980 | 2019-01-30 | US20190234015A1 | 2019-08-01 | Kosuke CHIDATE; Masakazu OHASHI; Toshiyuki MIYABAYASHI |
| A treatment liquid composition for ink jet pigment textile printing according to the invention is used by being attached to a fabric and contains a cationic compound, a nonionic fluorine-based surfactant, a resin particle, and water. | ||||||
| 45 | METHOD OF MAKING PLASTIC ARTICLE | US15500877 | 2015-07-28 | US20170218132A1 | 2017-08-03 | Cornelis Johannes G. M van PEER; Dirk Aart NOORDEGRAAF |
| A method of making a plastic article is disclosed. According to this method, a plastic article is formed from a thermoplastic composition that includes a first polymer component that is (i) a poly(siloxane-carbonate) copolymer, (ii) a poly(aliphatic ester)-polycarbonate having soft block ester units, derived from monomers including an alpha, omega C6-20 aliphatic dicarboxylic acid or derivative thereof, a dihydroxyaromatic compound, and a carbonate source, (iii) a thermoplastic polyurethane, (iv) a thermoplastic polyurethane, or a combination comprising any of the foregoing. An additive such as a photochromic dye is then loaded into the plastic article by contacting a surface of the article with supercritical fluid carbon dioxide comprising the additive dissolved or dispersed therein. | ||||||
| 46 | Dyeing and printing hydrophobic fiber in aqueous sulfonyl carbamic acid-type dyestuff solutions | US3708258D | 1971-06-28 | US3708258A | 1973-01-02 | VON DER ELTZ H; GUNTHER D; VOLLMANN H; KRELL K; MATTERSTOCK K |
| PROCESS FOR THE DYEING AND PRINTING OF HYDROPHOBIC FIBER MATERIALS BY TREATING THE GOODS IN THE PRESENCE OF AN ACID DONOR AT TEMPERATURES ABOVE 50* C. WITH AQUEOUS SOLUTIONS OF DYESTUFFS HAVING THE GENERAL FORMULA
F-X-CO-N(-ME)-SO3-ME WHEREIN F REPRESENTS THE RADICAL OF AN ORGANIC DYESTUFF WATER-INSOLUBLE PER SE, X REPRESENTS AN --O--, A --S-OR --NR-- BRIDGE MEMBER (R=A HYDROGEN ATOM OR AN ALKYL, ARYL, ACYL OR ALKYL OR ARYLSULFONYL GROUP) AND ME IS AN ALKALI METAL OR AMMONIUM ION. |
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| 47 | Process for the coloring of materials based on cellulose acetate employing,as carrier,cyanoalkylation products | US3513493D | 1967-09-27 | US3513493A | 1970-05-26 | PERRONIN JEAN; ZOGU ISKENDER GALAL |
| 48 | Dyeing cellulose esters and ethers | US2972935 | 1935-07-03 | US2037910A | 1936-04-21 | HOWARD KNIGHT ARTHUR |
| 49 | Process for dyeing or coloring cellulose esters and cellulose ethers | US1437535 | 1935-04-02 | US2031356A | 1936-02-18 | FRANZ ACKERMANN |
| 50 | Manufacture of new dyestuffs and the application thereof | US32321128 | 1928-12-01 | US1935205A | 1933-11-14 | HOLLAND ELLIS GEORGE |
| 51 | Treatment of materials made of or containing cellulose derivatives | US17501427 | 1927-03-12 | US1883350A | 1932-10-18 | HENRY DREYFUS |
| 285,641. British Celanese, Ltd., and Olpin, H. C. Feb. 9, 1927. Samples furnished. Anthraquinone derivatives.-Sulphuric esters of anthraquinonylamino alcohols, which are dyestuffs for organic substitution products of cellulose, e.g. cellulose esters and ethers, and for animal fibres, are made by treating the corresponding alcohols with sulphuric acid or oleum; or by the action of sulphuric esters of aminoalcohols on leuco oxyanthraquinones, e.g. the leuco compounds of 1-oxy-, 1 : 4-dioxy-, 1 : 4 : 5- trioxy or 1 : 4 : 5 : 8-tetraoxy-anthraquinone, followed by oxidation of the leuco body; or by replacement of chlor, nitro, methoxy &c. groups by treatment with sulphuric esters of aminoalcohols, e.g. #-aminoethyl alcohol. The anthraquinonylamino alcohols, for treatment with sulphuric acid or oleum, may be obtained by treating amino or mono-substituted amino derivatives of anthraquinone or substituted anthraquinones with halohydrins, e.g. ethylene, propylene or glyceryl chlorhydrins, epichlorhydrin, or chlorbutylene glycol, or with alkylene oxides, e.g. ethylene or propylene oxide, or with oxyaldehydes or ketones, or by replacement of chlor, nitro, hydroxy, methoxy &c. groups by treatment with an amino alcohol. The sulphuric esters of 1-#-oxyethylamino-, 1-#-oxyethylamino-2 (and 4)- methyl-, 1-#-oxyethylamino-4-oxy (and amino)-, 1-#-oxyethylamino-2-brom-4-amino-, and 1 : 4- and 1: 5-di-#-oxyethylamino-anthraquinones are specified. | ||||||
| 52 | Treatment of materials made of or containing cellulose derivatives | US41945730 | 1930-01-08 | US1855131A | 1932-04-19 | HENRY DREYFUS |
| 285,641. British Celanese, Ltd., and Olpin, H. C. Feb. 9, 1927. Samples furnished. Anthraquinone derivatives.-Sulphuric esters of anthraquinonylamino alcohols, which are dyestuffs for organic substitution products of cellulose, e.g. cellulose esters and ethers, and for animal fibres, are made by treating the corresponding alcohols with sulphuric acid or oleum; or by the action of sulphuric esters of aminoalcohols on leuco oxyanthraquinones, e.g. the leuco compounds of 1-oxy-, 1 : 4-dioxy-, 1 : 4 : 5- trioxy or 1 : 4 : 5 : 8-tetraoxy-anthraquinone, followed by oxidation of the leuco body; or by replacement of chlor, nitro, methoxy &c. groups by treatment with sulphuric esters of aminoalcohols, e.g. #-aminoethyl alcohol. The anthraquinonylamino alcohols, for treatment with sulphuric acid or oleum, may be obtained by treating amino or mono-substituted amino derivatives of anthraquinone or substituted anthraquinones with halohydrins, e.g. ethylene, propylene or glyceryl chlorhydrins, epichlorhydrin, or chlorbutylene glycol, or with alkylene oxides, e.g. ethylene or propylene oxide, or with oxyaldehydes or ketones, or by replacement of chlor, nitro, hydroxy, methoxy &c. groups by treatment with an amino alcohol. The sulphuric esters of 1-#-oxyethylamino-, 1-#-oxyethylamino-2 (and 4)- methyl-, 1-#-oxyethylamino-4-oxy (and amino)-, 1-#-oxyethylamino-2-brom-4-amino-, and 1 : 4- and 1: 5-di-#-oxyethylamino-anthraquinones are specified. | ||||||
| 53 | Dyeing of materials made of or containing cellulose derivatives | US25073028 | 1928-01-30 | US1735963A | 1929-11-19 | HENRY DREYFUS |
| 285,641. British Celanese, Ltd., and Olpin, H. C. Feb. 9, 1927. Samples furnished. Anthraquinone derivatives.-Sulphuric esters of anthraquinonylamino alcohols, which are dyestuffs for organic substitution products of cellulose, e.g. cellulose esters and ethers, and for animal fibres, are made by treating the corresponding alcohols with sulphuric acid or oleum; or by the action of sulphuric esters of aminoalcohols on leuco oxyanthraquinones, e.g. the leuco compounds of 1-oxy-, 1 : 4-dioxy-, 1 : 4 : 5- trioxy or 1 : 4 : 5 : 8-tetraoxy-anthraquinone, followed by oxidation of the leuco body; or by replacement of chlor, nitro, methoxy &c. groups by treatment with sulphuric esters of aminoalcohols, e.g. #-aminoethyl alcohol. The anthraquinonylamino alcohols, for treatment with sulphuric acid or oleum, may be obtained by treating amino or mono-substituted amino derivatives of anthraquinone or substituted anthraquinones with halohydrins, e.g. ethylene, propylene or glyceryl chlorhydrins, epichlorhydrin, or chlorbutylene glycol, or with alkylene oxides, e.g. ethylene or propylene oxide, or with oxyaldehydes or ketones, or by replacement of chlor, nitro, hydroxy, methoxy &c. groups by treatment with an amino alcohol. The sulphuric esters of 1-#-oxyethylamino-, 1-#-oxyethylamino-2 (and 4)- methyl-, 1-#-oxyethylamino-4-oxy (and amino)-, 1-#-oxyethylamino-2-brom-4-amino-, and 1 : 4- and 1: 5-di-#-oxyethylamino-anthraquinones are specified. | ||||||
| 54 | Dyeing of materials made of or containing cellulose derivatives | US17501227 | 1927-03-12 | US1735960A | 1929-11-19 | HENRY DREYFUS |
| 285,641. British Celanese, Ltd., and Olpin, H. C. Feb. 9, 1927. Samples furnished. Anthraquinone derivatives.-Sulphuric esters of anthraquinonylamino alcohols, which are dyestuffs for organic substitution products of cellulose, e.g. cellulose esters and ethers, and for animal fibres, are made by treating the corresponding alcohols with sulphuric acid or oleum; or by the action of sulphuric esters of aminoalcohols on leuco oxyanthraquinones, e.g. the leuco compounds of 1-oxy-, 1 : 4-dioxy-, 1 : 4 : 5- trioxy or 1 : 4 : 5 : 8-tetraoxy-anthraquinone, followed by oxidation of the leuco body; or by replacement of chlor, nitro, methoxy &c. groups by treatment with sulphuric esters of aminoalcohols, e.g. #-aminoethyl alcohol. The anthraquinonylamino alcohols, for treatment with sulphuric acid or oleum, may be obtained by treating amino or mono-substituted amino derivatives of anthraquinone or substituted anthraquinones with halohydrins, e.g. ethylene, propylene or glyceryl chlorhydrins, epichlorhydrin, or chlorbutylene glycol, or with alkylene oxides, e.g. ethylene or propylene oxide, or with oxyaldehydes or ketones, or by replacement of chlor, nitro, hydroxy, methoxy &c. groups by treatment with an amino alcohol. The sulphuric esters of 1-#-oxyethylamino-, 1-#-oxyethylamino-2 (and 4)- methyl-, 1-#-oxyethylamino-4-oxy (and amino)-, 1-#-oxyethylamino-2-brom-4-amino-, and 1 : 4- and 1: 5-di-#-oxyethylamino-anthraquinones are specified. | ||||||
| 55 | of basel | US1704637D | US1704637A | 1929-03-05 | ||
| 56 | Process of dyeing cellulose derivatives | US7739925 | 1925-12-28 | US1692492A | 1928-11-20 | HEINZ EICHWEDE; FRICH FISCHER; ERICH MULLER CARL |
| 57 | Process for dyeing cellulose esters and ethers | US17219527 | 1927-03-02 | US1662514A | 1928-03-13 | SMITH HORSFALL RONALD; GORDON LAWRIE LESLIE; JAMES HILL |
| 58 | Process of dyeing cellulose ethers | US6802725 | 1925-11-09 | US1599748A | 1926-09-14 | HEINZ EICHWEDE; ERICH FISCHER |
| 59 | Process of dyeing | US75245724 | 1924-11-26 | US1575324A | 1926-03-02 | WALTER DUISBERG; WINFRIED HENTRICH |
| 60 | Process of dyeing. | US1905243808 | 1905-02-02 | US794314A | 1905-07-11 | RICHARD BERNHARD |
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